Canonical Allele Identifier: PA102509
Gene: GFAP HGNC NCBI

Linked Data

ClinVar Variation Id: 16173
ClinVar RCV Id: RCV000017556 RCV000056878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002046.1:p.Arg88Ser
CA217182
NM_002055.5:c.262C>A